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http://dx.doi.org/10.5012/bkcs.2008.29.1.043

The Inhibitory Effect of New Hydroxamic Acid Derivatives on Melanogenesis  

Baek, Heung-Soo (R & D Center, AmorePacific Corporation)
Rho, Ho-Sik (R & D Center, AmorePacific Corporation)
Yoo, Jae-Won (R & D Center, AmorePacific Corporation)
Ahn, Soo-Mi (R & D Center, AmorePacific Corporation)
Lee, Jin-Young (R & D Center, AmorePacific Corporation)
Lee, Jeong-A (R & D Center, AmorePacific Corporation)
Kim, Min-Kee (R & D Center, AmorePacific Corporation)
Kim, Duck-Hee (R & D Center, AmorePacific Corporation)
Chang, Ih-Seop (R & D Center, AmorePacific Corporation)
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Abstract
The aim of present study was to examine the inhibitory effects of hydroxamic acid derivatives on the melanogenesis. We found that hydroxamic acid moiety was important for anti-melanogenic activity. Compounds 1a and 1b strongly inhibited melanin synthesis via deactivation of tyrosinase. Hydroxamic acid has metal ion chelating ability which is similar to that kojic acid, however, anti-tyrosinase mechanism of compounds 1a and 1b was different from that of kojic acid. They showed noncompetitive inhibition kinetics
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1 Penalver, M. J.; Hiner, A. N. P.; Rodriguez-Lopez, J. N.; Garcia- Canovas, F.; Tudela, J. Biochim. Biophys. Acta 2002, 1597, 140   DOI   ScienceOn
2 Fenoll, L. G.; Rodriguez-Lopez, J. N.; Garcia-Sevilla, F.; Garcia- Ruiz, P. A.; Varon, R.; Garcia-Canovas, F.; Tudela, J. Biochim. Biophys. Acta 2001, 1548, 1   DOI   ScienceOn
3 Ohyama, Y.; Mishima, Y. Fragrance J. 1990, 6, 53
4 Cho, S. J.; Roh, J. S.; Sun, W. S.; Kim, S. H.; Park, K. D. Bioorg. Med. Chem. Lett. 2006, 16, 2682   DOI   ScienceOn
5 Khatib, S.; Nerya, O.; Musa, R.; Shmuel, M.; Tamir, S.; Vaya, J. Bioorg. Med. Chem. 2005, 13, 433   DOI   ScienceOn
6 Curto, E. V.; Kwong, C.; Hermerdorfer, H.; Glatt, H.; Santis, C.; Virador, V.; Hearing, V. J.; Dooley, T. P. Biochem. Pharmacol. 1999, 57, 663   DOI   ScienceOn
7 Kubo, I.; Kinst-Hori, I.; Chaudhuri, S. K.; Kubo, Y.; Sanchez, Y.; Ogura, T. Bioorg. Med. Chem. 2000, 8, 1749   DOI   ScienceOn
8 Rich, P. R.; Wiegand, N. K.; Blum, H.; Moore, A. L.; Bonner, W. D. Biochim. Biophys. Acta 1978, 525, 325   DOI   ScienceOn
9 Reddy, A. S.; Kumar, M. S.; Reddy, G. R. Tetrahedron Lett. 2000, 41, 6285   DOI   ScienceOn
10 Pomerantz, S. H. J. Biol. Chem. 1963, 238, 2351
11 Rho, H. S.; Baek, H. S.; Kim, D. H.; Chang, I. S. Bull. Korean Chem. Soc. 2006, 27, 584   DOI   ScienceOn
12 Pirrung, M. C.; Tumey, L. N.; McClerren, A. L.; Raetz, C. R. H. J. Am. Chem. Soc. 2003, 125, 1575   DOI   ScienceOn
13 Denicola, A.; Souza, J. M.; Gatti, R. M.; Augusto, O.; Radi, R. Free Radic. Biol. Med. 1995, 19, 11   DOI   ScienceOn
14 Vanjari, H.; Pande, R. J. Pharm. Biomed. Anal. 2003, 33, 783   DOI   ScienceOn
15 Makris, D. P.; Rossiter, J. T. Food Chemistry 2002, 77, 177   DOI   ScienceOn
16 Farkas, E.; Enyedy, E. A.; Micera, G.; Garribba, E. Polyhedron 2000, 19, 1727   DOI   ScienceOn
17 Shin, N.-H.; Ryu, S. Y.; Choi, E. J.; Kang, S.-H.; Chang, I.-M.; Min, K. R.; Kim, Y. Biochem. Biophys. Res. Commun. 1998, 243, 801   DOI   ScienceOn
18 Taira, J.; Miyagi, C.; Aniya, Y. Biochem. Pharmacol. 2002, 63, 1019   DOI   ScienceOn
19 Shi, Y.; Chen, Q.-X.; Wang, Q.; Song, K.-K.; Qiu, L. Food Chemistry 2005, 92, 707   DOI   ScienceOn